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Thinking Healthy Program-Technology Assisted (THP-TA)

Technology-assisted Cognitive-behaviour Therapy Delivered by Peers Versus Standard Cognitive Behaviour Therapy Delivered by Community Health Workers for Perinatal Depression: A Cluster Randomised Controlled Non-inferiority Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05353491
Acronym
THP-TA
Enrollment
980
Registered
2022-04-29
Start date
2022-06-13
Completion date
2024-09-30
Last updated
2024-11-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression, Postpartum, Perinatal Depression

Keywords

Perinatal depression, Perinatal anxiety, perinatal mental health conditions, electronic CBT, CBT, task shifting, low-resourced settings, task sharing, Thinking Healthy Programme, LMIC, Technology-assisted, peers, community health workers

Brief summary

Background The Thinking Healthy Program (THP) is an evidence based task-shifted low intensity psychosocial intervention, recommended by the World Health Organization for the treatment of perinatal depression. The investigators developed a technology-assisted version of Thinking Healthy Program (THP-TA) which allows peers to deliver the THP, while ensuring minimal resources for training of delivery agents and ensuring adequate fidelity. Method This is a non-inferiority, pragmatic cluster randomized controlled trial designed to test the primary hypothesis that technology assisted delivery of THP is not worse than THP intervention delivered by community health workers, in increasing perinatal depression remission rates at 3 months postnatal. In addition, this study will also test the effectiveness of the THP-TA in improving recovery from perinatal depression at 6 months postpartum, quality of life and social support. This study also aims to evaluate the cost-effectiveness of the THP-TA.

Interventions

BEHAVIORALTechnology assisted Thinking Healthy Program (THP-TA)

A technology adapted version of the Thinking Healthy Program (THP) delivered by peers using multimedia android based app.

BEHAVIORALStandard Thinking Healthy Program

This intervention paper-based manual delivered by lady health workers ie government employed community health workers with health training background.

Sponsors

Shifa Tameer-e-Millat University
CollaboratorOTHER
University of Liverpool
CollaboratorOTHER
Human Development Research Foundation, Pakistan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Pregnant women with current major depressive episode in their second or third trimester (4 to 8 months of pregnancy). 2. Aged 18 years and above 3. Intent to stay in the study area for at least 1 year.

Exclusion criteria

1. Women requiring inpatient care for any reason (medical or psychiatric) as determined by their primary health care professional 2. Those who do not comprehend Urdu language will be excluded.

Design outcomes

Primary

MeasureTime frameDescription
Remission rates of perinatal depression3 months postnatalRemission rates from perinatal depression among the trial participants will be based on clinical diagnostic criteria based on the Structured Clinical Interview for the DSM-IV Axis (SCID) module. The SCID will be employed at baseline and 3 months postnatal.

Secondary

MeasureTime frameDescription
Change in severity of perinatal depressive symptoms3 months and 6 months postnatalSeverity of perinatal depressive symptoms will be measured using the Patient Health Questionnaire-9 items assessed at baseline, 3 months and 6 months postnatal. Score on this scale ranges from 0 to 27, with higher scores indicating increased severity.
Change in severity of perinatal anxiety symptoms3 months and 6 months postnatalSeverity of perinatal anxiety symptoms will be measured using the Generalized anxiety Disorder-7 scale assessed at baseline, 3 months and 6 months postnatal. Score on this scale ranges from 0 to 21, with higher scores indicating increased severity.
Change in maternal Quality of Life3 months and 6 months postnatalChange in maternal quality of life will be measured using the EuroQuality of Life scale (EQ-5D-3L), at baseline, 3 months and 6 months postnatal. It is a valid and reliable scale to quantify health status across 5 dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression.
Change in disability using the World Health Organization Disability Assessment Schedule 2.03 months and 6 months postnatalThis World Health Organization Disability Assessment Schedule 2.0 questionnaire assesses disability due to health conditions or illnesses (chronic or acute) including mental and emotional health problems. It is a valid and reliable instrument that generates domain-specific scores for six different functioning domains: i) cognition ii) mobility iii) self-care iv) getting along v) life activities (household and work/school) and vi) participation. It will be employed at baseline, 3 and 6 months postnatal.
Service use and costsPregnancy through to 6 months postnatalService use will be measured using Client Service Receipt Inventory (CSRI), including costs of healthcare services used, details and costs of medications and wider health service utilization and economic costs at 3 months and 6 months postnatal.
Infant nutrition/breastfeeding3 months and 6 months postnatalUsing 24-hour recall WHO breastfeeding practices tool, we will quantify percentage of infants being exclusively breastfed at 3 months and 6 months postnatal.
Sustained remission rates of perinatal depression3 months and 6 months postnatalSustained remission rates from perinatal depression among the trial participants will be based on clinical diagnostic criteria based on the Structured Clinical Interview for the DSM-IV Axis (SCID) module, assessed at baseline, 3 and 6 months postnatal.
Infant Immunization Status3 months and 6 months postnatalImmunization status of the infant will be assessed using a categorical question assessing completely or incompletely immunized as per the Expanded Programme on Immunization program in Pakistan, at 3 months and 6 months postnatal.
Maternal Social support3 months and 6 months postnatalMultidimensional Scale of Perceived Social Support (MSPSS) will be used to assess the perceived levels of social support among the intervention recipients at baseline, 3 months and 6 months postnatal, from three sources: family, friends and significant other. It comprises of 12 items, scores on which can be summed together with higher scores corresponding to better social support.
Parental time spent in play with the infant3 months and 6 months postnatalParental time spent in play with the infant will be assessed at 3 months and 6 months postnatal.
Diarrheal episodes among infants3 months and 6 months postnatalNumber of episodes of diarrheal episodes among infants will be assessed using the WHO criteria and definitions, at 3 months and 6 months postnatal
Acute upper respiratory tract infections among infants3 months and 6 months postnatalNumber of episodes of acute upper respiratory tract infections among infants will be assessed using the WHO criteria and definitions, at 3 months and 6 months postnatal
Family planning practices3 months and 6 months postnatalTo ascertain family planning practices, categorical questions will be asked regarding the use of contraception during the postpartum period.

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026